Chemoenzymatic elaboration of the Raper-Mason pathway unravels the structural diversity within eumelanin pigments

Melanin is a central polymer in living organisms, yet our understanding of its molecular structure remains unresolved. Here, we apply a biosynthetic approach to explore the composite structures accessible in one type of melanin, eumelanin. Using a combination of solid-state NMR, dynamic nuclear pola...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Chemical science (Cambridge) Ročník 11; číslo 3; s. 7836 - 7841
Hlavní autoři: Ni, Qing Zhe, Sierra, Brianna N, La Clair, James J, Burkart, Michael D
Médium: Journal Article
Jazyk:angličtina
Vydáno: Cambridge Royal Society of Chemistry 14.08.2020
The Royal Society of Chemistry
Témata:
ISSN:2041-6520, 2041-6539
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:Melanin is a central polymer in living organisms, yet our understanding of its molecular structure remains unresolved. Here, we apply a biosynthetic approach to explore the composite structures accessible in one type of melanin, eumelanin. Using a combination of solid-state NMR, dynamic nuclear polarization, and electron microscopy, we reveal how a variety of monomers are enzymatically polymerized into their corresponding eumelanin pigments. We demonstrate how this approach can be used to unite structure with an understanding of enzymatic activity, substrate scope, and the regulation of nanostructural features. Overall, this data reveals how intermediate metabolites of the Raper-Mason metabolic pathway contribute to polymerization, allowing us to revisit the original proposal of how eumelanin is biosynthesized. Melanin is a central polymer in living organisms, yet our understanding of its molecular structure remains unresolved.
Bibliografie:10.1039/d0sc02262d
Electronic supplementary information (ESI) available. See DOI
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:2041-6520
2041-6539
DOI:10.1039/d0sc02262d